Self-Templated Formation of P2-type K0.6CoO2 Microspheres for High Reversible Potassium-Ion Batteries

Layered metal oxides have been widely used as the best cathode materials for commercial lithium-ion batteries and are being intensively explored for sodium-ion batteries. However, their application to potassium-ion batteries (PIBs) is hampered because of the poor cycling stability and low rate capab...

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Published inNano letters Vol. 18; no. 2; pp. 1522 - 1529
Main Authors Deng, Tao, Fan, Xiulin, Luo, Chao, Chen, Ji, Chen, Long, Hou, Singyuk, Eidson, Nico, Zhou, Xiuquan, Wang, Chunsheng
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 14.02.2018
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Summary:Layered metal oxides have been widely used as the best cathode materials for commercial lithium-ion batteries and are being intensively explored for sodium-ion batteries. However, their application to potassium-ion batteries (PIBs) is hampered because of the poor cycling stability and low rate capability due to the larger ionic size of K+ than of Li+ or Na+. Herein, a facile self-templated strategy was used to synthesize unique P2-type K0.6CoO2 microspheres that consist of aggregated primary nanoplates as PIB cathodes. The unique K0.6CoO2 microspheres with aggregated structure significantly enhanced the kinetics of the K+ intercalation/deintercation and also minimized the parasitic reactions between the electrolyte and K0.6CoO2. The P2-K0.6CoO2 microspheres demonstrated a high reversible capacity of 82 mAh g–1 at 10 mA g–1, high rate capability of 65 mAh g–1 at 100 mA g–1, and long cycle life (87% capacity retention over 300 cycles). The high reversibility of the P2-K0.6CoO2 full cell paired with a hard carbon anode further demonstrated the feasibility of PIBs. This work not only successfully demonstrates exceptional performance of P2-type K0.6CoO2 cathodes and microspheres K0.6CoO2∥hard carbon full cells, but also provides new insights into the exploration of other layered metal oxides for PIBs.
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USDOE Office of Science (SC), Basic Energy Sciences (BES)
SC0001160
ISSN:1530-6984
1530-6992
1530-6992
DOI:10.1021/acs.nanolett.7b05324